List of variants in gene NRXN1 reported as likely benign for chromosomal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001330078.2(NRXN1):c.3365-110075G>A	rs189873392	0.00970
NM_001330078.2(NRXN1):c.4217-16A>C	rs74520052	0.00964
NM_001330078.2(NRXN1):c.4176T>C (p.Asp1392=)	rs201135028	0.00016
NM_001330078.2(NRXN1):c.3365-109899A>G	rs562219421	0.00012
NM_001330078.2(NRXN1):c.2625T>C (p.Asn875=)	rs764347791	0.00001
NM_138735.4(NRXN1):c.49GGC[11] (p.Gly17[11])	rs750165040

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